Metoclopramide Hydrochloride
- Product NDC
- 67296-1810
- 11-digit product format
- 672961810
- Labeler code
- 67296
- Product ID
- 67296-1810_b33846f4-473a-0bdb-e053-2a95a90a0383
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoclopramide Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA071250
- Marketing category
- ANDA
- Marketing start
- 2011-08-22
- Marketing end
- 2021-10-31
- Substance
- METOCLOPRAMIDE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1810-7 | 67296181007 | 21 TABLET in 1 BOTTLE (67296-1810-7) | 21 tablet | 2011-08-22 | 2021-10-31 | No | No | Current |